Canonical Allele Identifier: CA771673892

Gene: HNF1B

Linked Data

• dbSNP Id: rs1486163459
• gnomAD v3: 17-37739425-G-GT
• gnomAD v4: 17-37739425-G-GT
• MyVariant Identifiers: chr17:g.37739425_37739426insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37739425_37739426insT , CM000679.2:g.37739425_37739426insT	GRCh38
NC_000017.10:g.36099416_36099417insT , CM000679.1:g.36099416_36099417insT	GRCh37
NC_000017.9:g.33173529_33173530insT	NCBI36
NG_013019.2:g.10681_10682insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.544+14_544+15insA MANE Select	ENSP00000480291.1:n.544+14_544+15insA
ENST00000613727.4:c.544+14_544+15insA	ENSP00000477524.1:n.544+14_544+15insA
ENST00000614313.4:c.544+14_544+15insA	ENSP00000482529.1:n.544+14_544+15insA
ENST00000617272.4:c.544+14_544+15insA	ENSP00000478682.1:n.544+14_544+15insA
ENST00000617811.4:c.544+14_544+15insA	ENSP00000480291.1:n.544+14_544+15insA
ENST00000620125.1:c.544+14_544+15insA	ENSP00000481245.1:n.544+14_544+15insA
ENST00000621123.4:c.544+14_544+15insA	ENSP00000482711.1:n.544+14_544+15insA
NM_000458.3:c.544+14_544+15insA	NP_000449.1:n.544+14_544+15insA
NM_001165923.3:c.544+14_544+15insA	NP_001159395.1:n.544+14_544+15insA
NM_001304286.1:c.544+14_544+15insA	NP_001291215.1:n.544+14_544+15insA
XM_011525160.1:c.544+14_544+15insA	XP_011523462.1:n.544+14_544+15insA
XM_011525161.1:c.544+14_544+15insA	XP_011523463.1:n.544+14_544+15insA
XM_011525162.1:c.544+14_544+15insA	XP_011523464.1:n.544+14_544+15insA
XM_011525163.1:c.544+14_544+15insA	XP_011523465.1:n.544+14_544+15insA
XM_011525164.1:c.544+14_544+15insA	XP_011523466.1:n.544+14_544+15insA
XM_011525162.2:c.544+14_544+15insA	XP_011523464.1:n.544+14_544+15insA
XM_011525163.2:c.544+14_544+15insA	XP_011523465.1:n.544+14_544+15insA
NM_000458.4:c.544+14_544+15insA MANE Select	NP_000449.1:n.544+14_544+15insA
NM_001165923.4:c.544+14_544+15insA	NP_001159395.1:n.544+14_544+15insA
NM_001304286.2:c.544+14_544+15insA	NP_001291215.1:n.544+14_544+15insA